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Commercial newswire·CN·

48周减重近20%,胃肠道耐受性优异!翰森制药双偏向型GLP-1/GIP受体激动剂奥莱泊肽Ⅲ期研究数据闪耀EASD大会

上海 2026年10月2日 /美通社/ -- 2026年9月28日至10月2日,欧洲糖尿病研究协会(EASD)年会在意大利米兰召开。翰森制药原研双偏向型胰高血糖素样肽-1/葡萄糖依赖性促胰岛素多肽(GLP-1/GIP)受体激动剂——奥莱泊肽(Olatorepatide,代号HS-20094),以突破性摘要(LBA)口头报告形式公布中国减重Ⅲ期 LIGHTEN 研究结果,该研究于2026年3月达成主要终点。 报告显示,奥莱泊肽具有显著的减重疗效和优异的胃肠道耐受性:15mg组48周平均减重可达19.3%且未达平台,腰围平均降幅可达16.0cm;胃肠道不良事件发生率明显低于目前同类药物已发表数据,恶心发生率平均小于8%,呕吐发生率平均小…

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